Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K33/00—Medicinal preparations containing inorganic active ingredients
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K33/00—Medicinal preparations containing inorganic active ingredients
  • A61K33/24—Heavy metals; Compounds thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K33/00—Medicinal preparations containing inorganic active ingredients
  • A61K33/24—Heavy metals; Compounds thereof
  • A61K33/32—Manganese; Compounds thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K33/00—Medicinal preparations containing inorganic active ingredients
  • A61K33/24—Heavy metals; Compounds thereof
  • A61K33/34—Copper; Compounds thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P19/00—Drugs for skeletal disorders
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/04—Centrally acting analgesics, e.g. opioids
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Definitions

• the present invention relates to a pharmaceutical composition suitable for influencing the reticuloendothelic system and for treating mucoviscidosis an& chronic pain syndromes deriving from degenerative locomotor diseases or accompanying diseases of tumorous origin, and a process for preparing the same.
• Hungarian patent specification No. 176,202 and British patent specification No. 2,022,998 describe a pharmaceutical composition suitable for influencing the reticuloendothelic system (RES), i.e. the tissue system built up from different tissue types, situated at different anatomical positions or organs of the human or animal organism.
• RES reticuloendothelic system
• the said composition comprises
• potassium sodium tartrate potassium sodium tartrate
• the said composition is prepared by dissolving the components in aqueous medium, mixing the same with pharmaceutically acceptable carriers, diluents and/or excipients, then transforming the mixture thus obtained into a pharmaceutical composition in a manner known per se.
• boric acid is used as boron compound; sodium fluoride or vanadium trifluoride is used as fluorine compound; magnesium sulfate or magnesium chloride or the hydrate thereof is used as magnesium compound; ammonium vanadate or vanadium trifluoride is used as vanadium compound; manganese sulfate or manganese chloride or the hydrate thereof is used as manganese compound; iron(II)- or iron(III)-sulfate or the hydrate thereof is used as iron compound; cobalt chloride or cobalt sulfate or the hydrate thereof is used as cobalt compound; nickel chloride or nickel sulfate or the hydrate thereof is used as nickel compound; copper(II)-sulfate or the hydrate thereof is used as copper compound; zinc sulfate or the hydrate thereof is used as zinc compound; ammonium molybdenate or sodium molybdenate is used as molybdenum compound.
• disodium salt is used as tetrahalofluorescein salt
• disodium salt of ethylenediaminetetraacetic acid salt is used as ethylenediaminetetraacetic acid salt
• distilled water is used to make up the aqueous medium.
• the object of the present invention is to provide a pharmaceutical composition enabling the treatment of mucoviscidosis and chronic pain syndromes accompanying tumorous diseases or deriving from degenerative locomotor disorders, in addition to exhibiting the advantageous properties of the above-mentioned composition.
• the invention is based on the recognition that the above object can be achieved if the 2',4',5',7'-tetrahalofluorescein salt is omitted from the above-identified composition, while the composition is supplemented with succinic acid and L-(+)-tartaric acid.
• the composition thus obtained is suitable for the treatment of the above pain syndroms.
• the invention is based on the further recognition that by changing the components of the composition in the above manner, the composition thus obtained potentiates the effect of the conventional pain-killers, such as morphine, used for the treatment of chronic pain syndromes accompanying the tumorous diseases, i.e. the amount and the disadvantageous side-effects of the conventional pain-killers can be reduced, and it the tolerance threshold and the degree of addiction are favorably influenced.
• the conventional pain-killers such as morphine
• the invention is based on the further recognition that the advantageous properties of the composition described in the above Hungarian and British patent specifications remain practically unchanged if the lower limit of the weight ratio of certain components is reduced.
• the present invention relates to a pharmaceutical composition suitable for influencing the reticuloendothelic system and for the treatment of mucoviscidosis and chronic pain syndromes deriving from degenerative locomotor diseases or accompanying diseases of tumorous origin.
• the said pharmaceutical composition comprises
• L-(+)-tartaric acid wherein the mass ratio of the boron compound : fluorine compound : magnesium compound : vanadium compound : manganese compound : iron compound : cobalt compound : nickel compound : copper compound : zinc compound molybdenum compound : glycine : glycerol : L-(+)-ascorbic acid : succinic acid : ethylenediaminetetraacetic acid salt : potassium sodium tartrate : L-(+)-tartaric acid is 0.01-1:0.01-1:0.2-3:0.01-0.6:0.02:-2:0.15-6:0.002-1:0.01:2:0.01-1:0.1-3:0.001-0.8:0.1-2:0.2-8:0.01-2:0.001-2:0.01-3-:0.01-10:00.1-2.
• the said composition is prepared by dissolving the above components in aqueous medium, then transforming the mixture thus obtained together with one or more pharmaceutically acceptable diluents and/or excipients into a pharmaceutical composition in a manner known per se.
• the pharmaceutical composition according to the invention --similarly to the pharmaceutical composition described in the above-mentioned Hungarian and British patent specifications--is based substantially on water, i.e. the components can be dissolved and mixed in aqueous medium.
• composition according to the invention may comprise dissolution-promoting agents, preferably ethanol; buffers suitable for adjusting the desired, pharmaceutically acceptable pH, preferably hydrochloric acid or sulfuric acid; conventional pharmaceutical carriers, diluents and excipients.
• the concentration of components i)-viii) may vary within about 0.001 to 10% by weight/volume.
• the pharmaceutical composition provided by the invention may be prepared from various complexes which form together a more complicated complex when combined in an aqueous solution while keeping their water-soluble character.
• the aqueous solution obtained may be concentrated and the concentrate can be absorbed in a suppository mass to produce suppositories or pessaries.
• the pharmaceutical composition of the invention comprises boric acid as boron compound (preferably in an amount of 0.01 to 1.0% by weight/volume); sodium fluoride or vanadium trifluoride as fluorine compound (preferably in an amount of 0.01 to 1.0% by weight/volume); magnesium sulfate or magnesium chloride or the hydrate thereof as magnesium compound (preferably in an amount of 0.2 to 3.0% by weight/volume); ammonium vanadate or vanadium trifluoride as vanadium compound (preferably in an amount of 0.001 to 0.6% by weight/volume); manganese sulfate hydrate or manganese chloride tetrahydrate as manganese compound (preferably in an amount of 0.02 to 2.0% by weight/volume); iron(II)-sulfate heptahydrate or iron(III)-sulfate as iron compound (preferably in an amount of 0.15 to 6.0% by weight/volume); cobalt chloride hexahydrate or cobalt sulfate heptahydrate as cobalt
• the preferable concentration ranges of the other components of the pharmaceutical composition according to the invention are as follows:
• the preferable amount of ethanol (suitably of a concentration of 96% by volume) used as dissolution-promoting agent is 0.05 to 10.0% by weight/volume
• the preferable amount of the pharmaceutically acceptable acid, preferably hydrochloric acid or sulfuric acid, used for adjusting the pH of the solution is 0.05 to 1.0% by weight/volume.
• the pH of the pharmaceutical composition of the invention is preferably 1.9 to 4.0. 1 N sulfuric acid or hydrochloric acid is preferably used for adjusting the pH.
• composition according to the present invention can be administered orally, in the form of drops, or rectally or intravaginally, in the form of suppository or pessary.
• a pharmaceutical composition suitable for rectal or vaginal administration is preferably prepared by evaporating the aqueous solution to syrupy consistency and letting it to be absorbed in a suppository mass.
• the suppositories or pessaries are prepared from this mass in a way conventionally used in the pharmaceutical industry.
• the suppository mass is preferably prepared from cocoa-butter, carnauba wax or gelatine.
• 100 l of pharmaceutical composition is prepared as follows.
• the pH is adjusted to 1.9-4 with L-(+)-ascorbic acid.
• the volume of the solution being in the tank is supplemented to 98 l with distilled water.
• the pH of the solution is measured: it must be between 1.9 and 4. If the pH is above 4.0, it is adjusted to about 3.0 by the addition of further amounts of L-ascorbic acid. Finally the volume of the solution is supplemented to 100 liters.
• the solution thus obtained is left to stand for 12 to 24 hours. In the meantime the solution clarifies, its color turns to yellowish green. After quality control the solution can be formulated.
• Example 1 The process of Example 1 is followed except that the amounts of starting materials are chosen in such a manner that 100 ml of the ready-made solution comprise the following amounts of the components:
• Example 1 The process of Example 1 is followed except that the amounts of starting materials are chosen in such a manner that 100 ml of the ready-made solution comprise the following amounts of the components:
• Example 1 The process of Example 1 is followed except that the amount of starting materials is chosen in such a manner that 100 ml of the ready-made solution comprise the following amounts of the components:
• the patients being the subjects of the tests were male and female of different age. They received the composition according to the invention in solution form (1 ml corresponds to about 18 drops).
• the drops comprising the composition were administered in tea or soft drink.
• the patients were also administered 100 to 300 mg of ascorbic acid per day in the form of tablets or an aqueous solution, depending on the number of drops received.
• the patients suffering from gastric anacidity were optionally administered acid, too.
• Example 1 The composition of Example 1 was administered to adult patients in the following doses:
• the test covered 156 patients from which 76 patients (Group I) received effective composition, while 80 patients (Group II) were administered placebo. Improvement was observed in Group I with 57 patients (75%) and in Group II with 26 patients (32.5%). In Groups I and II the condition of 19 (25%) and 54 (67.5%) patients, respectively, remained constant.
• Mucoviscidosis is a congenital illness based on genetic lesion and is considered as an incurable disease even today. Its most conspicuous manifestation is that the product of the glands becomes highly viscous, contrary to the product of the normal glands. Therefore, the thick discharge produced by the glands adhere to the surface of the lungs and respiratory tracks covered by raucous membrane, it cannot be discharged spontaneously. The accumulated discharge and the pathogens dwelling in it will result in permanent inflammation which can lead to the destruction of the lungs. In the digestive tract the most severe consequence is the insufficient enzyme level in the duodenum due to the condensed pancreatic fluid which results in decreased digestion and utilization of the nutritive substances. As a result, the patients have abundant, undigested stool and still suffer from chronic lack of energy.
• the lifetime treatment is focused on the dissolution of the thick discharge and the substitution of the missing enzymes and vitamins. Nevertheless, not all insufficiencies can be solved completely even in spite of the most careful treatment. In addition, the susceptibility to infections is also higher.
• the test was started on 40 children suffering from mucoviscidosis, from which 5 children gave up the taking of the composition of the invention. Thus, the results relate to the treatment of only 35 children. The age of the children varied between 3 and 18 years.
• composition according to Example 3 was administered for 6 months in a daily dose of 1 drop per kg body weight.
• the change of the iron and zinc content in the blood serum of the patients was measured and it was found that the zinc and iron levels increased in the case of 32 (91%) and 18 (51%) patients, respectively, and played with high probability a significant role in the improvement of the patients.
• An other favorable result was that also the ferritin content increased in the blood serum of 25 (71%) patients.
• composition according to the invention ensures very favorable clinical results in the treatment of mucoviscidosis and chronic pain syndromes deriving from degenerative locomotor diseases or accompanying diseases of tumorous origin.
• the dose of the pharmaceutical composition of the invention depends on the state, body weight and illness of the patient.
• the daily dose may vary between 5 and 500 drops, and it amounts suitably to 20-150 drops, preferably to 40-80 drops per day.

Landscapes

• Health & Medical Sciences (AREA)
• Chemical & Material Sciences (AREA)
• Medicinal Chemistry (AREA)
• Pharmacology & Pharmacy (AREA)
• Life Sciences & Earth Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Inorganic Chemistry (AREA)
• Epidemiology (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Engineering & Computer Science (AREA)
• Pain & Pain Management (AREA)
• Rheumatology (AREA)
• Biomedical Technology (AREA)
• Neurology (AREA)
• Neurosurgery (AREA)
• Physical Education & Sports Medicine (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
• Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
• Medicinal Preparation (AREA)
• Medicines Containing Material From Animals Or Micro-Organisms (AREA)
• Saccharide Compounds (AREA)
• Steroid Compounds (AREA)
• Catching Or Destruction (AREA)
• Percussion Or Vibration Massage (AREA)
• Measurement And Recording Of Electrical Phenomena And Electrical Characteristics Of The Living Body (AREA)
• Electrotherapy Devices (AREA)
• Circuits Of Receivers In General (AREA)

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Related Child Applications (1)

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ID=10959658

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Cited By (6)

Families Citing this family (25)

Citations (2)

• 1991
  • 1991-07-24 HU HU912492A patent/HU207799B/hu unknown
  • 1991-07-26 US US07/736,314 patent/US5312629A/en not_active Expired - Fee Related
• 1992
  • 1992-06-26 HR HR920192A patent/HRP920192B1/xx not_active IP Right Cessation
  • 1992-07-21 PL PL92295352A patent/PL169684B1/pl not_active IP Right Cessation
  • 1992-07-22 RO RO92-01006A patent/RO109505B1/ro unknown
  • 1992-07-23 RU SU925052277A patent/RU2093160C1/ru active
  • 1992-07-24 CA CA002074639A patent/CA2074639C/en not_active Expired - Fee Related
  • 1992-07-24 JP JP4217451A patent/JP2673852B2/ja not_active Expired - Fee Related
  • 1992-07-24 FI FI923364A patent/FI923364A/fi not_active Application Discontinuation
  • 1992-07-24 KR KR1019920013264A patent/KR100234855B1/ko not_active IP Right Cessation
  • 1992-07-24 CZ CS922326A patent/CZ281672B6/cs unknown
  • 1992-07-24 EP EP92112643A patent/EP0524633B1/en not_active Expired - Lifetime
  • 1992-07-24 SK SK2326-92A patent/SK278944B6/sk unknown
  • 1992-07-24 BG BG96686A patent/BG61250B1/bg unknown
  • 1992-07-24 SI SI19929200155A patent/SI9200155A/sl unknown
  • 1992-07-24 AT AT92112643T patent/ATE178213T1/de not_active IP Right Cessation
  • 1992-07-24 DE DE69228777T patent/DE69228777T2/de not_active Expired - Fee Related
  • 1992-09-02 YU YU81092A patent/YU48243B/sh unknown
• 1993
  • 1993-11-12 US US08/152,052 patent/US5405620A/en not_active Expired - Fee Related

Patent Citations (2)

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